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Insecta: Phasmatodea) and Their Phylogeny
insects Article Three Complete Mitochondrial Genomes of Orestes guangxiensis, Peruphasma schultei, and Phryganistria guangxiensis (Insecta: Phasmatodea) and Their Phylogeny Ke-Ke Xu 1, Qing-Ping Chen 1, Sam Pedro Galilee Ayivi 1 , Jia-Yin Guan 1, Kenneth B. Storey 2, Dan-Na Yu 1,3 and Jia-Yong Zhang 1,3,* 1 College of Chemistry and Life Science, Zhejiang Normal University, Jinhua 321004, China; [email protected] (K.-K.X.); [email protected] (Q.-P.C.); [email protected] (S.P.G.A.); [email protected] (J.-Y.G.); [email protected] (D.-N.Y.) 2 Department of Biology, Carleton University, Ottawa, ON K1S 5B6, Canada; [email protected] 3 Key Lab of Wildlife Biotechnology, Conservation and Utilization of Zhejiang Province, Zhejiang Normal University, Jinhua 321004, China * Correspondence: [email protected] or [email protected] Simple Summary: Twenty-seven complete mitochondrial genomes of Phasmatodea have been published in the NCBI. To shed light on the intra-ordinal and inter-ordinal relationships among Phas- matodea, more mitochondrial genomes of stick insects are used to explore mitogenome structures and clarify the disputes regarding the phylogenetic relationships among Phasmatodea. We sequence and annotate the first acquired complete mitochondrial genome from the family Pseudophasmati- dae (Peruphasma schultei), the first reported mitochondrial genome from the genus Phryganistria Citation: Xu, K.-K.; Chen, Q.-P.; Ayivi, of Phasmatidae (P. guangxiensis), and the complete mitochondrial genome of Orestes guangxiensis S.P.G.; Guan, J.-Y.; Storey, K.B.; Yu, belonging to the family Heteropterygidae. We analyze the gene composition and the structure D.-N.; Zhang, J.-Y. -
24Th Annual Philippine Biodiversity Symposium
24th Annual Philippine Biodiversity Symposium University of Eastern Philippines Catarman, Northern Samar 14-17 April 2015 “Island Biodiversity Conservation: Successes, Challenges and Future Direction” th The 24 Philippine Biodiversity Symposium organized by the Biodiversity Conservation Society of the Philippines (BCSP), hosted by the University of Eastern Philippines in Catarman, Northern Samar 14-17 April 2015 iii iv In Memoriam: William Langley Richardson Oliver 1947-2014 About the Cover A Tribute to William Oliver he design is simply 29 drawings that represent the endemic flora and fauna of the Philip- illiam Oliver had spent the last 30 years working tirelessly pines, all colorful and adorable, but the characters also all compressed and crowded in a championing threatened species and habitats in the small area or island much like the threat of the shrinking habitats of the endemics in the Philippines and around the world. William launched his islands of the Philippines. This design also attempts to provide awareness and appreciation W wildlife career in 1974 at the Jersey Wildlife Preservation Trust. In Tof the diverse fauna and flora found only in the Philippines, which in turn drive people to under- 1977, he undertook a pygmy hog field survey in Assam, India and from stand the importance of conserving these creatures. There are actually 30 creatures when viewing then onwards became a passionate conservationist and defender the design, the 30th being the viewer to show his involvement and responsibility in conservation. of the plight of wild pigs and other often overlooked animals in the Philippines, Asia and across the globe. He helped establish the original International Union for Conservation of Nature’s Pigs and Peccaries Specialist Group in 1980 at the invitation of British conservationist, the late Sir Peter Scott. -
The Early Evolution of Biting–Chewing Performance in Hexapoda
Chapter 6 The Early Evolution of Biting–Chewing Performance in Hexapoda Alexander Blanke Abstract Insects show a plethora of different mandible shapes. It was advocated that these mandible shapes are mainly a function of different feeding habits. This hypothesis was tested on a larger sampling of non-holometabolan biting–chewing insects with additional tests to understand the interplay of mandible function, feeding guild, and phylogeny. The results show that at the studied systematic level, variation in mandible biting–chewing effectivity is regulated to a large extent by phylogenetic history and the configuration of the mandible joints rather than the food preference of a given taxon. Additionally, lineages with multiple mandibular joints such as primary wingless hexapods show a wider functional space occupation of mandibular effectivity than dicondylic insects (¼ silverfish + winged insects) at significantly different evolutionary rates. The evolution and occupation of a compa- rably narrow functional performance space of dicondylic insects is surprising given the low effectivity values of this food uptake solution. Possible reasons for this relative evolutionary “stasis” are discussed. 6.1 Introduction Insecta sensu lato (¼ Hexapoda) display a high diversity of mouthpart shapes within the early evolved lineages which started to radiate approximately 479 million years ago (Misof et al. 2014). These shape changes were described qualitatively and were often stated to relate mainly to the type of food consumed (Yuasa 1920; Isely 1944; Evans and Forsythe 1985; Chapman and de Boer 1995). To the knowledge of the author, this and related statements regarding mouthpart mechanics being shaped by functional demands have never been tested in a quantitative framework. -
Insect Egg Size and Shape Evolve with Ecology but Not Developmental Rate Samuel H
ARTICLE https://doi.org/10.1038/s41586-019-1302-4 Insect egg size and shape evolve with ecology but not developmental rate Samuel H. Church1,4*, Seth Donoughe1,3,4, Bruno A. S. de Medeiros1 & Cassandra G. Extavour1,2* Over the course of evolution, organism size has diversified markedly. Changes in size are thought to have occurred because of developmental, morphological and/or ecological pressures. To perform phylogenetic tests of the potential effects of these pressures, here we generated a dataset of more than ten thousand descriptions of insect eggs, and combined these with genetic and life-history datasets. We show that, across eight orders of magnitude of variation in egg volume, the relationship between size and shape itself evolves, such that previously predicted global patterns of scaling do not adequately explain the diversity in egg shapes. We show that egg size is not correlated with developmental rate and that, for many insects, egg size is not correlated with adult body size. Instead, we find that the evolution of parasitoidism and aquatic oviposition help to explain the diversification in the size and shape of insect eggs. Our study suggests that where eggs are laid, rather than universal allometric constants, underlies the evolution of insect egg size and shape. Size is a fundamental factor in many biological processes. The size of an 526 families and every currently described extant hexapod order24 organism may affect interactions both with other organisms and with (Fig. 1a and Supplementary Fig. 1). We combined this dataset with the environment1,2, it scales with features of morphology and physi- backbone hexapod phylogenies25,26 that we enriched to include taxa ology3, and larger animals often have higher fitness4. -
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Checklist of the terrestrial and freshwater arthropods of French Polynesia (Chelicerata; Myriapoda; Crustacea; Hexapoda) Thibault RAMAGE 9 quartier de la Glacière, F-29900 Concarneau (France) and Service du Patrimoine naturel, Muséum national d’Histoire naturelle, case postale 41, 57 rue Cuvier, F-75231 Paris cedex 05 (France) [email protected] Published on 30 June 2017 urn:lsid:zoobank.org:pub:51C2E5A2-0132-48B6-A747-94F37C349B36 Ramage T. 2017. — Checklist of the terrestrial and freshwater arthropods of French Polynesia (Chelicerata; Myriapoda; Crustacea; Hexapoda). Zoosystema 39 (2): 213-225. https://doi.org/10.5252/z2017n2a3 ABSTRACT An annotated checklist for the terrestrial and freshwater arthropods of French Polynesia is presented. Compiled with the help of 48 experts and based on published records, it comprises 3025 valid species names belonging to the classes of Hexapoda Blainville, 1816 (2556 species), Chelicerata Heymons, 1901 (36 7 species), Myriapoda Latreille, 1802 (22 species) and Crustacea Pennant, 1777 (80 species). Reported are 1841 taxa from the Society Islands, followed by the Marquesas Islands with 1198 taxa, KEY WORDS the Austral Islands with 609 taxa, the Tuamotu Islands with 231 taxa and the Gambier Islands with Species database, 186 taxa. The specificity of this fauna and the analysis of each class and order are discussed. The level endemism, of endemism is particularly high, 61% of the known species, with non-native species representing biogeography, speciation, 13% of the overall species count. The threats to the native fauna and flora of French Polynesia and threats to endemic species. particularly to endemic insect species are detailed. RÉSUMÉ Liste de référence des arthropodes terrestres et d’eau douce de Polynésie française (Chelicerata; Myriapoda; Crustacea; Hexapoda). -
Embioptera: Oligotomidae) in Japan
BioInvasions Records (2018) Volume 7, Issue 2: 211–214 Open Access DOI: https://doi.org/10.3391/bir.2018.7.2.15 © 2018 The Author(s). Journal compilation © 2018 REABIC Rapid Communication First record of the web spinner Haploembia solieri (Rambur, 1842) (Embioptera: Oligotomidae) in Japan Tomonari Nozaki1,*, Naoyuki Nakahama2, Wataru Suehiro1 and Yusuke Namba3 1Laboratory of Insect Ecology, Graduate School of Agriculture, Kyoto University, Kitashirakawa-Oiwakecho, Sakyo-ku, Kyoto 606-8502, Japan 2Laboratory of Plant Evolution and Biodiversity, Graduate school of Arts and Sciences, The University of Tokyo, Meguro-Ku, Tokyo, 153-8902, Japan 3Honmachi, Toyonaka, Osaka, 560-0021, Japan Author e-mails: [email protected] (TN), [email protected] (NN), [email protected] (WS), [email protected] (YN) *Corresponding author Received: 31 January 2018 / Accepted: 30 April 2018 / Published online: 21 May 2018 Handling editor: Angeliki Martinou Abstract The impact of biological invasions is unpredictable, and hence it is important to provide information at the earliest stage of invasion. This is the first report of the web spinner Haploembia solieri (Rambur, 1842) (Insecta: Embioptera) in Japan. We found this species in the Port of Kobe, on an artificial island in Hyogo Prefecture. The locality is clearly distant from its known distribution; H. solieri is native in the Mediterranean region and introduced into the United States. In our surveys, 90 individuals were collected, but no males. This is also the first report of H. solieri in East Asia. Because we observed the H. solieri population in the fall of 2016 and early summer of 2017, this species may have been able to overwinter in Japan. -
Using Mitochondrial Genomes to Infer Phylogenetic Relationships
bioRxiv preprint doi: https://doi.org/10.1101/164459; this version posted August 22, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Using mitochondrial genomes to infer phylogenetic relationships 2 among the oldest extant winged insects (Palaeoptera) 3 Sereina Rutschmanna,b,c*, Ping Chend, Changfa Zhoud, Michael T. Monaghana,b 4 Addresses: 5 aLeibniz-Institute of Freshwater Ecology and Inland Fisheries (IGB), Müggelseedamm 301, 12587 6 Berlin, Germany 7 bBerlin Center for Genomics in Biodiversity Research, Königin-Luise-Straße 6-8, 14195 Berlin, 8 Germany 9 cDepartment of Biochemistry, Genetics and Immunology, University of Vigo, 36310 Vigo, Spain 10 dThe Key Laboratory of Jiangsu Biodiversity and Biotechnology, College of Life Sciences, Nanjing 11 Normal University, Nanjing 210046, China 12 13 *Correspondence: Sereina Rutschmann, Department of Biochemistry, Genetics and Immunology, 14 University of Vigo, 36310 Vigo, E-mail: [email protected] 15 16 17 18 1 bioRxiv preprint doi: https://doi.org/10.1101/164459; this version posted August 22, 2017. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 19 Abstract 20 Phylogenetic relationships among the basal orders of winged insects remain unclear, in particular the 21 relationship of the Ephemeroptera (mayflies) and the Odonata (dragonflies and damselflies) with the 22 Neoptera. -
Downloaded and Searched Using
bioRxiv preprint doi: https://doi.org/10.1101/453514; this version posted November 17, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. 1 Title: Bacterial contribution to genesis of the novel germ line determinant oskar 2 3 Authors: Leo Blondel1, Tamsin E. M. Jones2,3 and Cassandra G. Extavour1,2* 4 5 Affiliations: 6 1. Department of Molecular and Cellular Biology, Harvard University, 16 Divinity Avenue, 7 Cambridge MA, USA 8 2. Department of Organismic and Evolutionary Biology, Harvard University, 16 Divinity 9 Avenue, Cambridge MA, USA 10 3. Current address: European Bioinformatics Institute, EMBL-EBI, Wellcome Genome 11 Campus, Hinxton, Cambridgeshire, UK 12 13 * Correspondence to [email protected] 14 15 Abstract: New cellular functions and developmental processes can evolve by modifying 16 existing genes or creating novel genes. Novel genes can arise not only via duplication or 17 mutation but also by acquiring foreign DNA, also called horizontal gene transfer (HGT). Here 18 we show that HGT likely contributed to the creation of a novel gene indispensable for 19 reproduction in some insects. Long considered a novel gene with unknown origin, oskar has 20 evolved to fulfil a crucial role in insect germ cell formation. Our analysis of over 100 insect 21 Oskar sequences suggests that Oskar arose de novo via fusion of eukaryotic and prokaryotic 22 sequences. This work shows that highly unusual gene origin processes can give rise to novel 23 genes that can facilitate evolution of novel developmental mechanisms. -
Chec List First Records of Four Species of Webspinners (Insecta
Check List 10(6): 1565–1569, 2014 © 2014 Check List and Authors Chec List ISSN 1809-127X (available at www.biotaxa.org/cl) Journal of species lists and distribution N First records of four species of webspinners (Insecta: Embioptera) from Chhattisgarh, India ISTRIBUTIO D Kailash Chandra and Prosenjit Dawn* RAPHIC G * Corresponding Author. E-mail: [email protected] EO Zoological Survey of India, M- Block, New Alipore, Kolkata-700053, India G N O Abstract: Out of 32 species or subspecies known from India, four species, namely Oligotoma humbertiana (Saussure, 1896), Oligotoma OTES saundersii (Westwood, The present 1837) paper anddeals Oligotoma with the firstannandalei taxonomic Kapur account & Kripalani, on webspinners 1957 (family (Embioptera) Oligotomidae) of Chhattisgarh, and Pseudembia India. N setosa Ross, 1950 (family Embiidae) are reported for the first time from Chhattisgarh. DOI: 10.15560/10.6.1565 Among the small insect orders, Embioptera is a distinct, from India, but study of the literatures decreases the number monophyletic group with representatives distributed to 32. Hitherto, no work has been done on the Embioptera throughout warmer regions of the world (Miller et al. of Chhattisgarh state, which initiated the research presented 2012). Less than 400 valid species of this group are in this paper. Four species, Oligotoma humbertiana (Saussure, currently recorded but there are as many as undocumented 1896) (Figure1A), Oligotoma saundersii (Westwood, 1837) species (Miller 2009). (Figure1B), Oligotoma annandalei Kapur & Kripalani, 1957 Webspinners are medium sized (5 to 25 mm) insects (Figure1C), and Pseudembia setosa Ross, 1950 (Figure 1D) with a slender and campodeiform body. Mouth parts are newly recorded from this state. -
Aposthonia Krauss, 1911 (Embioptera: Oligotomidae) from Thailand, with Description of a New Species
Zootaxa 2937: 37–48 (2011) ISSN 1175-5326 (print edition) www.mapress.com/zootaxa/ Article ZOOTAXA Copyright © 2011 · Magnolia Press ISSN 1175-5334 (online edition) Aposthonia Krauss, 1911 (Embioptera: Oligotomidae) from Thailand, with description of a new species PISIT POOLPRASERT1,2, DUANGKHAE SITTHICHAROENCHAI2, BUNTIKA AREEKUL BUTCHER2 & CHARIYA LEKPRAYOON2,3 1Biological Science Program, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand 2Department of Biology, Faculty of Science, Chulalongkorn University, Bangkok, 10330, Thailand 3Corresponding author. E-mail: [email protected] Abstract Three embiid species of the genus Aposthonia Krauss (Oligotomidae) are recognized from Thailand (Aposthonia borneen- sis, A. ceylonica, A. problita sp. n.) and the new species is described. The distribution of the three species in Thailand is shown and keys to the males of 25 species of this genus and to females found in Thailand are provided. Key words: Aposthonia, Embioptera, Oligotomidae, Thailand Introduction The Embioptera (webspinners) is a small insect order in terms of the number of described species and genera, with approximately 2,000 species estimated to exist in the world (Ross 2000a). Most embiid species are small to medium sized, narrow-bodied insects and are easily recognized by the large, bulbous basal tarsomere on each fore- leg. They live in silk-lined galleries; the silk is produced by glands and spun when the silk is ejected through hol- low hair-like structures on the ventral surface of the basal tarsal segment. Webspinners feed entirely on vegetable matter such as outer bark, dead leaves and lichens. In general, the distribution of webspinners is restricted to the tropics and subtropics (Ross 1970, 2000a, 2007), but some representatives are occasionally also found in the warm temperate zones, probably as a result of recent artificial (anthropogenic) introduction through commerce. -
Evolutionary Morphology of the Antennal Heart in Stick and Leaf Insects (Phasmatodea) and Webspinners (Embioptera) (Insecta: Eukinolabia)
Zoomorphology https://doi.org/10.1007/s00435-021-00526-4 ORIGINAL PAPER Evolutionary morphology of the antennal heart in stick and leaf insects (Phasmatodea) and webspinners (Embioptera) (Insecta: Eukinolabia) Benjamin Wipfer1 · Sven Bradler2 · Sebastian Büsse3 · Jörg Hammel4 · Bernd R. Müller5 · Günther Pass6 Received: 28 January 2021 / Revised: 15 April 2021 / Accepted: 27 April 2021 © The Author(s) 2021 Abstract The morphology of the antennal hearts in the head of Phasmatodea and Embioptera was investigated with particular refer- ence to phylogenetically relevant key taxa. The antennal circulatory organs of all examined species have the same basic construction: they consist of antennal vessels that are connected to ampullae located in the head near the antenna base. The ampullae are pulsatile due to associated muscles, but the points of attachment difer between the species studied. All examined Phasmatodea species have a Musculus (M.) interampullaris which extends between the two ampullae plus a M. ampulloaorticus that runs from the ampullae to the anterior end of the aorta; upon contraction, all these muscles dilate the lumina of both ampullae at the same time. In Embioptera, only the australembiid Metoligotoma has an M. interampullaris. All other studied webspinners instead have a M. ampullofrontalis which extends between the ampullae and the frontal region of the head capsule; these species do not have M. ampulloaorticus. Outgroup comparison indicates that an antennal heart with a M. interampullaris is the plesiomorphic character state among Embioptera and the likely ground pattern of the taxon Eukinolabia. Antennal hearts with a M. ampullofrontalis represent a derived condition that occurs among insects only in some embiopterans. -
The Higher Classification of the Order Embioptera: a Cladistic Analysis
Cladistics (1996) 12:41±64 THE HIGHER CLASSIFICATION OF THE ORDER EMBIOPTERA: A CLADISTIC ANALYSIS Claudia A. Szumik Department of Entomology, American Museum of Natural History, Central Park West at 79th Street, New York, 10024, U.S.A. and CONICET, Facultad de Ciencias Naturales e Instituto Miguel Lillo, Miguel Lillo 205, 4000 S.M. de TucumaÂn, Argentina Received for publication 24 April 1994; accepted 24 July 1995 Abstract Ð A matrix of 41 Embiid taxa (representing the 8 formally recognized families of the Order) and 36 characters were cladistically analysed as a first attempt for understanding the higher classification of the Order Embioptera. The resulting trees were rooted with Clothodidae as the sister group of the other Embioptera. The results suggest that the current classification contains several artificial groups. With the rooting used, only Anisembiidae and Australembiidae are monophyletic. Embiidae is polyphyletic, as Australembiidae+ Notoligotomidae, Enveja (incertae sedis) and Oligotomidae+Teratembiidae appear within Embiidae, and the ªembiidº Microembia appears within Notoligotomidae. Oligotomidae is paraphyletic in terms of Teratembiidae. Four of the genera included in the analysis are paraphyletic: Mesembia, Chelicerca (in terms of Dactylocerca and Pelorembia), Aposthonia (in terms of Oligotoma), and Metoligotoma (in terms of Australembia). Pelorembia and Dactylocerca are synonymized with Chelicerca. 1996 The Willi Hennig Society Introduction The insect order Embioptera is a monophyletic group defined by several morphological and behavioral characters. The most striking apomorphy of these subsocial insects is their ability to produce silk in all instars from unicellular glands in the swollen first basitarsus (Barth, 1954; Alberti et al., 1976; Nagashima et al., 1991) and to use it to construct tunnels under bark, stones or soil.